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HEMO-VALVE

Page Type
Cleared 510(K)
510(k) Number
K955554
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1996
Days to Decision
90 days
Submission Type
Summary

HEMO-VALVE

Page Type
Cleared 510(K)
510(k) Number
K955554
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1996
Days to Decision
90 days
Submission Type
Summary